Powder Synthesis and Properties of Litao3 Ceramics ⇑ Tao Yang, Yan-Gai Liu , Lei Zhang, Mei-Ling Hu, Qian Yang, Zhao-Hui Huang, Ming-Hao Fang

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Powder Synthesis and Properties of Litao3 Ceramics ⇑ Tao Yang, Yan-Gai Liu , Lei Zhang, Mei-Ling Hu, Qian Yang, Zhao-Hui Huang, Ming-Hao Fang Advanced Powder Technology 25 (2014) 933–936 Contents lists available at ScienceDirect Advanced Powder Technology journal homepage: www.elsevier.com/locate/apt Original Research Paper Powder synthesis and properties of LiTaO3 ceramics ⇑ Tao Yang, Yan-gai Liu , Lei Zhang, Mei-ling Hu, Qian Yang, Zhao-hui Huang, Ming-hao Fang School of Materials Science and Technology, China University of Geosciences (Beijing), Beijing 100083, PR China article info abstract Article history: The LiTaO3 powders with sub micrometer grade grain size have been synthesized successfully using a Received 26 April 2013 molten salt method. Lithium tantalate began to form at 400 °C reaction temperature and transformed Received in revised form 8 January 2014 to pure phase without residual reactants when it was processed at 500 °C for 4 h in static air. The Accepted 17 January 2014 undoped LiTaO ceramics with a Curie temperature about 663 °C were obtained by pressureless sintering Available online 28 January 2014 3 at 1300 °C for 3 h. The relative dielectric constant (er) increases from 50 to 375 at temperature ranging from 30 to 663 °C and then decreases quickly as the temperature increases above 663 °C. The ceramics Keywords: shows a relative dielectric constant of 49.4, a dielectric loss factor (tand) of 0.007, a coercive field (Ec) Lithium tantalite ceramics of 28.66 kV/cm and a remnant polarization (Pr) of 32.48 C/cm2 at room temperature. Molten salt method l Sintering Ó 2014 The Society of Powder Technology Japan. Published by Elsevier B.V. and The Society of Powder Ferroelectric properties Technology Japan. All rights reserved. 1. Introduction new low temperature synthesis methods with high efficiency and productivity are required. LiTaO3 (LTO), as a promising electro-optic material with excel- Molten salt method has been reported as a highly efficient and lent ferroelectric, piezoelectric and pyroelectric properties as well low-cost technique for preparing ceramic materials based on the as large nonlinear optical coefficients, has led to a variety of re- reaction of the constituent oxides [15,16] and has numerous merits search fields including functionalized ceramics, optical wave such as high yield, relatively low calcination temperatures, high guides, modulators and surface acoustic wave devices [1–5]. Syn- phase purity and crystallinity, short reaction times. In this method, thesis of pure LTO crystalline materials with different shapes and a salt or eutectic molten salt, such as alkali chlorides, carbonates, sizes has attracted a great deal of interest with applications with hydroxides, and sulfates, are used as a reaction medium to intro- their unique electro-optical properties. Usually, conventional solid duce high diffusion rates between reactants. However, very few re- state synthesis method, using Li2CO3 and Ta2O5 as raw materials, ports focused on preparing LTO using the molten salt method. In requires processing temperatures above 1000 °C. It could introduce this work, pure polycrystalline LTO ceramics prepared by a pres- many intrinsic lithium deficiencies in lithium tantalate (LTO) due sureless sintering method involving powders that were synthes- to the evaporation of lithium at high synthesis temperatures, ised by molten salt method. To the best of our knowledge, this resulting great influences of their physical properties such as lat- undoped polycrystalline LTO ceramics have rarely been reported tice parameters, Curie temperature, absorption edge, coercive yet. fields, refractive indices and photorefractive optical damage resis- tance [6]. Therefore some wet chemical routes, such as hydrother- mal, colloid emulsion, sol–gel, co-precipitation, spray drying, 2. Experimental polymerized complex method, impregnation method [7–13], were Monohydrate lithium chloride (Sinopharm Chemical Reagent developed as promising alternatives for fabricating LiTaO3 powders in recently. Comparing to the conventional solid-state method, Co., Ltd., China) and potassium chloride (Xilong Chemical Industry these wet chemical techniques are operated at low temperature Co., Ltd., China) with molar ratio of 0.59:0.41 were used as eutectic and can obtain highly pure, homogeneous materials and control salt without further purification in this process, which have the the size and morphology of the particles effectively [14]. However, lowest eutectic temperature 353 °C (the data comes from FACT Salt wet chemical routes are time-consuming, operation-complicated, Phase Diagrams). The synthesis process was summarized briefly as costly and low-productivity. Consequently, these methods are dif- follows: 1.43 g lithium carbonate (Xilong Chemical Industry Co., Ltd., China), 8.57 g tantalum pentoxide (Ningxia Orient Tantalum ficult to apply for the commercialization of LiTaO3 materials and Industry Co., Ltd., China), 0.69 g monohydrate lithium chloride and 0.59 g potassium chloride were mixed and ball-milled for ⇑ Corresponding author. Tel./fax: +86 010 82322186. 12 h. After ball milling, the mixtures were calcined in a tube fur- E-mail address: [email protected] (Y.-g. Liu). nace for 4 h in air at various calcination temperatures ranging from 0921-8831/$ - see front matter Ó 2014 The Society of Powder Technology Japan. Published by Elsevier B.V. and The Society of Powder Technology Japan. All rights reserved. http://dx.doi.org/10.1016/j.apt.2014.01.011 934 T. Yang et al. / Advanced Powder Technology 25 (2014) 933–936 400 to 650 °C with the step of 50 °C, respectively, and then natu- is observed at temperature above 600 °C. The first endothermic rally cooled to room temperature. The heating rate of the furnace peak centered at 128.13 °C shown in the DSC curve is attributed was 5 °C minÀ1 when the temperature was below 200 °C and to the loss of crystal water in monohydrate lithium chloride, which 10 °C minÀ1 when the temperature was above 200 °C. The as-pre- is coincided with the TG analysis as previously mentioned. The DSC pared products were washed by hot deionized water for several curve exhibits the second endothermic peak at 354.43 °C because times to remove residual salts and then dried in a circulation oven of eutectic reaction of lithium chloride with potassium chloride. at 110 °C for 4 h. Then the powders were pressed into a disk with a The third endothermic peak associates to eutectic temperature at diameter of 10 mm and thickness of 2–3 mm and sintered at 417.18 °C of lithium carbonate, lithium chloride and potassium. A 1300 °C for 3 h. After polished, the as-sintered disc was coated by broad exothermic peak at round 480.88 °C corresponds to the reac- silver paste and heated at 550 °C for 0.5 h. tion between lithium and tantalum complex ions. The second exo- Thermogravimetry analysis (TG) and differential scanning col- thermic peak centered at 559.10 °C can be assigned to the orimeter (DSC, NETZSCH STA 449F3) were carried out to investi- crystallization of LiTaO3 without corresponding appreciable weight gate the weight loss and transition energy of mixtures as a loss in the TG curve. function of temperature at a heating rate of 10 °C/min. Phase iden- tification of the as-calcinated powders was characterized by X-ray 3.1.2. XRD analysis diffractometer (XRD model XD-3) using Cu Ka1 radiation The XRD patterns of powders calcined at a certain temperature (k = 0.15406 nm) at 40 kV and 40 mA. The XRD patterns were re- from the range between 400 °C and 650 °C for 4 h are shown in À1 corded in the 2h range of 20–80° at a scanning rate of 8° min Fig. 2. As shown in Fig. 2, the observed weak diffraction peaks of in steps of 0.02°. The morphology of the as-prepared samples LTO phase indicate that it can be synthesized at 400 °C. Numerous was examined by field emission scanning electron microscopy peaks of Ta2O5 were detected at this temperature while no Li2CO3 (FESEM, JSM-7001F) with an energy-dispersive X-ray spectrometer phase was detected because of the water extraction. It suggests (EDS, Oxford, Link ISIS). The powders were ultrasonically dispersed that molten salt can promote the transformation of starting mate- into absolute ethyl alcohol for 30 min and then the suspension was rials effectively at lower temperature. The diffraction peaks be- dropped onto a standard TEM copper grid. The microstructure was came sharper when the sintering temperature increased, examined using a high-resolution transmission electron micro- indicating that the increased temperatures promoted the crystalli- scope (HRTEM, FEI Tecnai G2 F20, USA). The relative dielectric con- zation and growth of LTO. With the raising of calcination temper- stant ( ) and the dielectric loss tangent (tand) were measured er ature (lower than 500 °C), the quantity of LiTaO3 was increased. examined a precision impedance analyser (Agilent 4294A). The Pure LTO phase was prepared by the LiCl–KCl molten-salt method P–E hysteresis curves were measured at room temperature using for 4 h calcination at of 500 °C. It is noting that this molten-salt a ferroelectric tester (Trek 609B). The temperature dependence of method can impede the evaporation of lithium and largely reduce relative dielectric constant was examined from 30 to 750 °Cat the intrinsic lithium deficiencies in LTO crystal compared with 1 MHz utilizing a furnace with an LCR analyser (TH2828S). conventional solid state reaction method using much high temper- atures (>1000 °C). Therefore, no diffraction peaks for other prod- ucts but only LTO were detected. All the X-ray diffraction 3. Results and discussion patterns of LTO are indexed well to the standard pattern of rhom- bohedral LiTaO (JCPDS Card No. 29-0836, space group R3c, 3.1. Powder characterization 3 a = b = 0.5153 nm, c = 1.3755 nm) and the corresponding average sizes of LTO crystallites prepared at 650 °C calculated using Scher- 3.1.1. TG-DSC analysis rer’s equation is 395 nm.
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